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Patients with chronic graft-versus-host disease often have skin problems like vitiligo and alopecia areata.

Autoimmune liver diseases are likely linked to certain skin conditions like vitiligo and psoriasis.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

A rare skin condition causes red and dark patches on the face and limbs.

The woman has a type of scarring hair loss with red bumps around hair follicles.

Trichoscopy helps distinguish Lichen Planopilaris from Frontal Fibrosing Alopecia by identifying unique hair loss patterns.

The woman has a scalp condition causing hair loss.

Trichoscopy helps effectively tell apart different types of patchy hair loss in Egyptian patients.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

Lichen planopilaris should be considered in diagnosing scarring hair loss in Black women.

Children with alopecia areata have different trichoscopic features than adults, including more empty follicular openings and pigtail hairs.

Natural killer cells play a key role in autoimmune skin diseases like pemphigus vulgaris.

Adipose tissue and eccrine gland displacement are common in certain alopecias but don't help differentiate between them.

The hair coat disorder in Schipperkes is similar to Alopecia X and involves increased androstenedione levels and hair cycle arrest.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

Different types of hair loss and gender affect facial heat patterns, which may help diagnose and treat hair loss.

Lupus erythematosus panniculitis on the scalp can cause unique geometric hair loss patterns.

Two patients with lupus had an unusual type of hair loss not typical for the disease but improved with treatment.

LC-OCT is an effective new method for diagnosing classic lichen planopilaris.

The study suggests a link between varicella-zoster virus and segmental vitiligo, with evidence of the virus disrupting skin pigment cells.

Two new signs, 'signet ring vessels' and 'hidden hairs,' help tell apart scalp psoriasis and seborrheic dermatitis.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

Recognizing perinevoid alopecia and concentric regrowth is important for diagnosing and treating alopecia areata.

The child was diagnosed with cutaneous leishmaniasis.

Yellow dots were the most common sign of alopecia areata found using trichoscopy.

A 42-year-old woman had a scalp lesion that didn't cause hair loss and showed specific changes under a microscope.

Trichoscopy is useful for detecting and monitoring androgenetic alopecia.

Microinflammation is more intense in smaller hair follicles and may be linked to hair loss.